Evaluación Radiológica de las Cardiopatias Congenitas. 1. Cardiopatías Congénitas; 2. Cardiopatías Congénitas Incidencia 8 de cada. Primer sitio Web en Argentina sobre cardiopatías congénitas.
|Published (Last):||5 March 2012|
|PDF File Size:||1.89 Mb|
|ePub File Size:||9.79 Mb|
|Price:||Free* [*Free Regsitration Required]|
Congenital heart disease caused by mutations in the transcription factor NKX A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Nat Genet, 13pp.
Genomic, 10pp. Clin Genet, 54pp.
Genética de las cardiopatías congénitas | Anales de Pediatría
The DiGeorge anomaly with renal agenesis in infants of mothers with diabetes. Prevalence of cardiovascular malformations and association with karyotypes in Turner’s syndrome.
Hum Genet, 90pp. Diagn Mol Pathol, congenitqspp. Pediatr Clin North Am, 37pp. A major involvement of the cardiovascular system in patients affected by Marfan syndrome: Am J Med Genet, 43pp. Interstitial deletion of 22q11 in DiGeorge syndrome de-tected by high resolution and molecular analysis. Am J Med Genet, 73pp.
CARDIOPATIAS CONGENITAS EN PEDIATRIA PDF
Am J Med Genet, 39pp. Deletions of 20p12 in Alagille syndrome: Eur J Pediatr,pp. Am J Med Genet, 37pp. Am J Med Genet, 70pp. Clin Genet, 29pp.
Am J Hum Genet, 64pp. Hypoparathyroidism as the major manifestation in two patients with 22q11 deletions. Toward a molecular understanding of congenital heart disease. CiteScore measures average citations received per document published.
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndrome. Nat Genet, 13pp. Hospital 12 de Cagdiopatias. Cardiac anomalies associated with a chromosome 22q11 deletion in patients with conotruncal anomaly face syndrome.
Adv Pediatr, 45pp. A deletion in chromosome 22 can cause DiGeorge syndrome. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.
Am J Hum Genet, 51pp. J Am Coll Cardiol, 23pp. Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p Deletions and microdeletions of 22q Nat Genet, 8pp. Thymic deficiency in an infant with a psdiatria t 18;22 q Phenotype of the Williams-Beuren syndrome associated with hemizygosity at the elastin locus. Prevalence of 22q11 microdeletions in Di-George and velocardiofacial syndromes: J Cardiovasc Electrophysiol, 10pp.
J Mol Cell Cardiol, 29pp. Am J Hum Genet, 56pp.
There was a problem providing the content you requested
Am J Med Genet, 65pp. Am J Med Genet, 73pp. Overweight and obesity in children treated for congenital We review current knowledge on the genetic etiology of congenital heart disease. Hum Mutat, 13pp. The DiGeorge anomaly as a develop-mental field defect. Alagille syndrome arteriohepatic dysplasia and del 20 p Molecular definition of the chromosome 7 deletion in Wi-lliams syndrome and parent-of-origin effects on growth.
J Mol Cell Cardiol, 29pp. Ultrasound Obstetr Gynecol, 10pp. Causes of dilated cardiomyopathy.